DK1963307T3 - 3- (4 - {[4- (4 - {[3- (3,3-Dimethyl-1-piperidinyl) propyl] oxy} phenyl) -1-piperidinyl] carbonyl} -1-naphthalenyl) propionic or propenoic acid as H1 and H3 receptor antagonists for the treatment of inflammatory and / or allergic disorders - Google Patents
3- (4 - {[4- (4 - {[3- (3,3-Dimethyl-1-piperidinyl) propyl] oxy} phenyl) -1-piperidinyl] carbonyl} -1-naphthalenyl) propionic or propenoic acid as H1 and H3 receptor antagonists for the treatment of inflammatory and / or allergic disordersInfo
- Publication number
- DK1963307T3 DK1963307T3 DK06841477.0T DK06841477T DK1963307T3 DK 1963307 T3 DK1963307 T3 DK 1963307T3 DK 06841477 T DK06841477 T DK 06841477T DK 1963307 T3 DK1963307 T3 DK 1963307T3
- Authority
- DK
- Denmark
- Prior art keywords
- piperidinyl
- naphthalenyl
- oxy
- propionic
- carbonyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Otolaryngology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0525897A GB0525897D0 (en) | 2005-12-20 | 2005-12-20 | Compounds |
| GB0623217A GB0623217D0 (en) | 2006-11-21 | 2006-11-21 | Compounds |
| PCT/EP2006/069943 WO2007071691A1 (en) | 2005-12-20 | 2006-12-19 | 3- (4-{ [4-(4-{ [3-(3, 3-dimethyl-1-piperidinyl) propyl] 0xy} phenyl) -1-piperidinyl] carbonyl }-1-naphthalenyl) propanoic or propenoic acid as h1 and h3 receptor antagonists for the treatment of inflammatory and/or allergic disorders |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DK1963307T3 true DK1963307T3 (en) | 2010-04-06 |
Family
ID=37845266
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK06841477.0T DK1963307T3 (en) | 2005-12-20 | 2006-12-19 | 3- (4 - {[4- (4 - {[3- (3,3-Dimethyl-1-piperidinyl) propyl] oxy} phenyl) -1-piperidinyl] carbonyl} -1-naphthalenyl) propionic or propenoic acid as H1 and H3 receptor antagonists for the treatment of inflammatory and / or allergic disorders |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US7989629B2 (en) |
| EP (2) | EP2157087A1 (en) |
| JP (2) | JP4445570B2 (en) |
| KR (1) | KR20080087102A (en) |
| AR (1) | AR058109A1 (en) |
| AT (1) | ATE449769T1 (en) |
| AU (1) | AU2006328512B2 (en) |
| BR (1) | BRPI0620218A2 (en) |
| CA (1) | CA2634391A1 (en) |
| CR (1) | CR10102A (en) |
| CY (1) | CY1110601T1 (en) |
| DE (1) | DE602006010737D1 (en) |
| DK (1) | DK1963307T3 (en) |
| EA (1) | EA014354B1 (en) |
| ES (1) | ES2337187T3 (en) |
| HK (1) | HK1120265A1 (en) |
| IL (1) | IL191967A0 (en) |
| MA (1) | MA30373B1 (en) |
| NO (1) | NO20082695L (en) |
| PE (1) | PE20071068A1 (en) |
| PL (1) | PL1963307T3 (en) |
| PT (1) | PT1963307E (en) |
| SI (1) | SI1963307T1 (en) |
| TW (1) | TW200730498A (en) |
| WO (1) | WO2007071691A1 (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2285803A4 (en) | 2008-05-23 | 2011-10-05 | Amira Pharmaceuticals Inc | 5-lipoxygenase-activating protein inhibitor |
| EP2448578A1 (en) | 2009-06-29 | 2012-05-09 | Glaxo Group Limited | New medical use |
| JP4785963B2 (en) | 2009-10-09 | 2011-10-05 | キヤノン株式会社 | Solid-state imaging device |
| WO2013151982A1 (en) | 2012-04-03 | 2013-10-10 | Arena Pharmaceuticals, Inc. | Methods and compounds useful in treating pruritus, and methods for identifying such compounds |
| MX2016014859A (en) | 2014-05-12 | 2017-06-27 | Glaxosmithkline Intellectual Property (No 2) Ltd | Pharmaceutical compositions comprising danirixin for treating infectious diseases. |
| KR101640756B1 (en) | 2014-10-28 | 2016-07-19 | 이종찬 | Drill assembling device for Endoscope cap for installing electronic drill |
| WO2019169082A1 (en) * | 2018-03-01 | 2019-09-06 | Ferox Therapeutics Llc | Methods of preventing and treating hypoglycemia in type 1 and type 2 diabetes patients |
| EP4125919A1 (en) | 2020-03-26 | 2023-02-08 | GlaxoSmithKline Intellectual Property Development Limited | Cathepsin inhibitors for preventing or treating viral infections |
Family Cites Families (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9127376D0 (en) | 1991-12-24 | 1992-02-19 | Wellcome Found | Amidino derivatives |
| WO1993019749A1 (en) | 1992-04-02 | 1993-10-14 | Smithkline Beecham Corporation | Compounds useful for treating allergic and inflammatory diseases |
| CA2135644C (en) | 1992-05-14 | 2009-01-27 | Elisabetta Vegeto | Mutated steroid hormone receptors, methods for their use and molecular switch for gene therapy |
| US5364791A (en) | 1992-05-14 | 1994-11-15 | Elisabetta Vegeto | Progesterone receptor having C. terminal hormone binding domain truncations |
| AU692892B2 (en) | 1994-06-15 | 1998-06-18 | Wellcome Foundation Limited, The | Enzyme inhibitors |
| MY117948A (en) | 1997-01-13 | 2004-08-30 | Glaxo Group Ltd | Nitride oxide synthase inhibitors. |
| DE19723722A1 (en) | 1997-05-30 | 1998-12-10 | Schering Ag | Nonsteroidal progestogens |
| WO1999016766A1 (en) | 1997-10-01 | 1999-04-08 | Kyowa Hakko Kogyo Co., Ltd. | Benzodioxole derivatives |
| US6506766B1 (en) | 1998-02-13 | 2003-01-14 | Abbott Laboratories | Glucocortiocoid-selective antinflammatory agents |
| CA2323771A1 (en) | 1998-03-14 | 1999-09-23 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Phthalazinone pde iii/iv inhibitors |
| GB9811599D0 (en) | 1998-05-30 | 1998-07-29 | Glaxo Group Ltd | Nitric oxide synthase inhibitors |
| CA2371273A1 (en) | 1999-05-04 | 2000-11-09 | Andrew Fensome | Tetracyclic progesterone receptor modulator compounds and methods |
| ES2165768B1 (en) | 1999-07-14 | 2003-04-01 | Almirall Prodesfarma Sa | NEW DERIVATIVES OF QUINUCLIDINE AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM. |
| CO5180649A1 (en) | 1999-09-01 | 2002-07-30 | Abbott Lab | ANTAGONISTS OF GLUCOCORTICOID RECEPTORS FOR THE TREATMENT OF DIABETES FOR THE TREATMENT OF DIABETES |
| OA11558A (en) | 1999-12-08 | 2004-06-03 | Advanced Medicine Inc | Beta 2-adrenergic receptor agonists. |
| NZ523958A (en) | 2000-08-05 | 2004-11-26 | Glaxo Group Ltd | 17.beta.-carbothioate 17.alpha.-arylcarbonyloxyloxy androstane derviative as anti-inflammatory agents |
| GB0031179D0 (en) | 2000-12-21 | 2001-01-31 | Glaxo Group Ltd | Nitric oxide synthase inhibitors |
| US6484903B2 (en) | 2001-01-09 | 2002-11-26 | Riverwood International Corporation | Carton with an improved dispensing feature in combination with a unique handle |
| GB0103630D0 (en) | 2001-02-14 | 2001-03-28 | Glaxo Group Ltd | Chemical compounds |
| WO2002070490A1 (en) | 2001-03-08 | 2002-09-12 | Glaxo Group Limited | Agonists of beta-adrenoceptors |
| EP1370521B1 (en) | 2001-03-22 | 2007-12-19 | Glaxo Group Limited | Formanilide derivatives as beta2-adrenoreceptor agonists |
| USRE44874E1 (en) | 2001-09-14 | 2014-04-29 | Glaxo Group Limited | Phenethanolamine derivatives for treatment of respiratory diseases |
| WO2003042160A1 (en) | 2001-11-13 | 2003-05-22 | Theravance, Inc. | Aryl aniline beta-2 adrenergic receptor agonists |
| ES2276038T3 (en) | 2002-01-14 | 2007-06-16 | Boehringer Ingelheim Pharmaceuticals Inc. | MIMETICS OF GLUCOCORTICOIDS, METHODS FOR OBTAINING THEM, PHARMACEUTICAL FORMULATIONS CONTAINING THEMSELVES AND USES OF THE SAME. |
| WO2003061651A1 (en) | 2002-01-22 | 2003-07-31 | The Regents Of The University Of California | Non-steroidal ligands for the glucocorticoid receptor, compositions and uses thereof |
| GB0204719D0 (en) | 2002-02-28 | 2002-04-17 | Glaxo Group Ltd | Medicinal compounds |
| EA008830B1 (en) | 2002-03-26 | 2007-08-31 | Бёрингер Ингельхайм Фармасьютиклз, Инк. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
| EP1490317A1 (en) | 2002-03-26 | 2004-12-29 | Boehringer Ingelheim Pharmaceuticals Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
| DE10215316C1 (en) | 2002-04-02 | 2003-12-18 | Schering Ag | Quinoline and isoquinoline derivatives, a pharmaceutical agent and their use as anti-inflammatory agents |
| EP1496892B1 (en) | 2002-04-11 | 2011-01-26 | Merck Sharp & Dohme Corp. | 1h-benzo(f)indazol-5-yl derivatives as selective glucocorticoid receptor modulators |
| JP2005523920A (en) | 2002-04-25 | 2005-08-11 | グラクソ グループ リミテッド | Phenetanolamine derivative |
| US7186864B2 (en) | 2002-05-29 | 2007-03-06 | Boehringer Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
| US7074806B2 (en) | 2002-06-06 | 2006-07-11 | Boehringer Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
| JP4503436B2 (en) | 2002-07-08 | 2010-07-14 | ファイザー・プロダクツ・インク | Glucocorticoid receptor modulators |
| PL375442A1 (en) | 2002-07-18 | 2005-11-28 | Bristol-Myers Squibb Company | Modulators of the glucocorticoid receptor and method |
| GB0217225D0 (en) | 2002-07-25 | 2002-09-04 | Glaxo Group Ltd | Medicinal compounds |
| ATE403648T1 (en) | 2002-08-21 | 2008-08-15 | Boehringer Ingelheim Pharma | SUBSTITUTED DIHYDROCINOLINES AS GLUCOCORTICOID MIMMETICS, METHOD FOR THE PRODUCTION THEREOF, PHARMACEUTICAL PREPARATIONS AND THEIR USE |
| GB0220730D0 (en) | 2002-09-06 | 2002-10-16 | Glaxo Group Ltd | Medicinal compounds |
| GB0230045D0 (en) | 2002-12-23 | 2003-01-29 | Glaxo Group Ltd | Compounds |
| PL375993A1 (en) | 2002-09-16 | 2005-12-12 | Glaxo Group Limited | Pyrazolo[3,4-b]pyridine compounds, and their use as phosphodiesterase inhibitors |
| JP4520309B2 (en) | 2002-09-20 | 2010-08-04 | メルク・シャープ・エンド・ドーム・コーポレイション | Octahydro-2-H-naphtho [1,2-f] indole-4-carboxamide derivatives as selective glucocorticoid receptor modulators |
| GB0224084D0 (en) * | 2002-10-16 | 2002-11-27 | Glaxo Group Ltd | Novel compounds |
| EP1554260A1 (en) | 2002-10-22 | 2005-07-20 | Glaxo Group Limited | Aryloxyalkylamine derivatives as h3 receptor ligands |
| JP2006506373A (en) | 2002-10-22 | 2006-02-23 | グラクソ グループ リミテッド | Pharmaceutical arylethanolamine compounds |
| GB0225030D0 (en) | 2002-10-28 | 2002-12-04 | Glaxo Group Ltd | Medicinal compounds |
| WO2004037773A1 (en) | 2002-10-28 | 2004-05-06 | Glaxo Group Limited | Phenethanolamine derivative for the treatment of respiratory diseases |
| GB0225540D0 (en) | 2002-11-01 | 2002-12-11 | Glaxo Group Ltd | Medicinal compounds |
| GB0225535D0 (en) | 2002-11-01 | 2002-12-11 | Glaxo Group Ltd | Medicinal compounds |
| GB0308333D0 (en) * | 2003-04-10 | 2003-05-14 | Glaxo Group Ltd | Novel compounds |
| TWI328009B (en) | 2003-05-21 | 2010-08-01 | Glaxo Group Ltd | Quinoline derivatives as phosphodiesterase inhibitors |
| PE20060272A1 (en) | 2004-05-24 | 2006-05-22 | Glaxo Group Ltd | (2R, 3R, 4S, 5R, 2'R, 3'R, 4'S, 5'S) -2.2 '- {TRANS-1,4-CYCLOHEXANODIYLBIS- [IMINO (2 - {[2- (1-METHYL- 1H-IMIDAZOL-4-IL) ETHYL] AMINO} -9H-PURIN-6,9-DIYL)]} BIS [5- (2-ETHYL-2H-TETRAZOLE-5-IL) TETRAHYDRO-3,4-FURANODIOL] AS AN A2A AGONIST |
| WO2006000398A1 (en) | 2004-06-28 | 2006-01-05 | Glaxo Group Limited | 2,3-benzoxazin derivatives as non-steroidal glucocorticoid receptor modulators |
| WO2006000401A1 (en) | 2004-06-28 | 2006-01-05 | Glaxo Group Limited | Substituted oxazines as glucocorticoid receptor modulators |
| GB0418045D0 (en) | 2004-08-12 | 2004-09-15 | Glaxo Group Ltd | Compounds |
| US7465795B2 (en) * | 2005-12-20 | 2008-12-16 | Astrazeneca Ab | Compounds and uses thereof |
| WO2007122156A1 (en) | 2006-04-20 | 2007-11-01 | Glaxo Group Limited | 2-substituted 4-benzylphthalazinone derivatives as histamine h1 and h3 antagonists |
-
2006
- 2006-12-18 AR ARP060105590A patent/AR058109A1/en not_active Application Discontinuation
- 2006-12-18 PE PE2006001620A patent/PE20071068A1/en not_active Application Discontinuation
- 2006-12-18 TW TW095147457A patent/TW200730498A/en unknown
- 2006-12-19 JP JP2008546432A patent/JP4445570B2/en not_active Expired - Fee Related
- 2006-12-19 US US12/158,185 patent/US7989629B2/en not_active Expired - Fee Related
- 2006-12-19 EP EP09176715A patent/EP2157087A1/en not_active Withdrawn
- 2006-12-19 AT AT06841477T patent/ATE449769T1/en active
- 2006-12-19 SI SI200630560T patent/SI1963307T1/en unknown
- 2006-12-19 DK DK06841477.0T patent/DK1963307T3/en active
- 2006-12-19 EP EP06841477A patent/EP1963307B1/en active Active
- 2006-12-19 WO PCT/EP2006/069943 patent/WO2007071691A1/en active Application Filing
- 2006-12-19 KR KR1020087015535A patent/KR20080087102A/en not_active Application Discontinuation
- 2006-12-19 AU AU2006328512A patent/AU2006328512B2/en not_active Ceased
- 2006-12-19 EA EA200801342A patent/EA014354B1/en not_active IP Right Cessation
- 2006-12-19 BR BRPI0620218-7A patent/BRPI0620218A2/en not_active IP Right Cessation
- 2006-12-19 PL PL06841477T patent/PL1963307T3/en unknown
- 2006-12-19 ES ES06841477T patent/ES2337187T3/en active Active
- 2006-12-19 CA CA002634391A patent/CA2634391A1/en not_active Abandoned
- 2006-12-19 PT PT06841477T patent/PT1963307E/en unknown
- 2006-12-19 DE DE602006010737T patent/DE602006010737D1/en active Active
-
2008
- 2008-06-05 IL IL191967A patent/IL191967A0/en unknown
- 2008-06-11 MA MA31023A patent/MA30373B1/en unknown
- 2008-06-11 NO NO20082695A patent/NO20082695L/en not_active Application Discontinuation
- 2008-06-20 CR CR10102A patent/CR10102A/en not_active Application Discontinuation
-
2009
- 2009-02-04 HK HK09101002.5A patent/HK1120265A1/en not_active IP Right Cessation
- 2009-06-12 JP JP2009140796A patent/JP2009235087A/en active Pending
-
2010
- 2010-02-19 CY CY20101100170T patent/CY1110601T1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US7989629B2 (en) | 2011-08-02 |
| KR20080087102A (en) | 2008-09-30 |
| BRPI0620218A2 (en) | 2011-11-01 |
| PT1963307E (en) | 2010-03-03 |
| SI1963307T1 (en) | 2010-03-31 |
| TW200730498A (en) | 2007-08-16 |
| PL1963307T3 (en) | 2010-05-31 |
| ATE449769T1 (en) | 2009-12-15 |
| EP1963307B1 (en) | 2009-11-25 |
| US20080312280A1 (en) | 2008-12-18 |
| EA014354B1 (en) | 2010-10-29 |
| EA200801342A1 (en) | 2008-12-30 |
| ES2337187T3 (en) | 2010-04-21 |
| CA2634391A1 (en) | 2007-06-28 |
| CR10102A (en) | 2008-09-22 |
| EP2157087A1 (en) | 2010-02-24 |
| MA30373B1 (en) | 2009-05-04 |
| JP4445570B2 (en) | 2010-04-07 |
| EP1963307A1 (en) | 2008-09-03 |
| PE20071068A1 (en) | 2007-12-13 |
| CY1110601T1 (en) | 2015-04-29 |
| JP2009235087A (en) | 2009-10-15 |
| IL191967A0 (en) | 2008-12-29 |
| NO20082695L (en) | 2008-09-16 |
| AU2006328512A1 (en) | 2007-06-28 |
| AR058109A1 (en) | 2008-01-23 |
| AU2006328512B2 (en) | 2011-06-23 |
| DE602006010737D1 (en) | 2010-01-07 |
| HK1120265A1 (en) | 2009-03-27 |
| WO2007071691A1 (en) | 2007-06-28 |
| JP2009520001A (en) | 2009-05-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DK1963307T3 (en) | 3- (4 - {[4- (4 - {[3- (3,3-Dimethyl-1-piperidinyl) propyl] oxy} phenyl) -1-piperidinyl] carbonyl} -1-naphthalenyl) propionic or propenoic acid as H1 and H3 receptor antagonists for the treatment of inflammatory and / or allergic disorders | |
| LTC1793824I2 (en) | New pharmaceutical compositions comprising 4- (4- (3- (4-chloro-3-trifluoromethylphenyl) ureido) -3-fluorophenoxy) pyridine-2-carboxylic acid for the treatment of hyperproliferative disorders | |
| ATE516272T1 (en) | 1,3-DISUBSTITUTED 4-(ARYL-X-PHENYL)-1H-PYRIDINE-2-ONE | |
| CY2016017I2 (en) | COMPOSITION FOR THE TREATMENT OF PULMONARY HYPERTENSION | |
| IL183827A0 (en) | Novel heterocyclic compounds useful for the treatment of inflammatory and allergic disorders | |
| NO20061420L (en) | 3 - [(2- (4-Hexyloxycarbonylamino-imino-methyl) -phenylamino] -methyl} -1-methyl-1H-benzimidazole-5-carbonyl) -pyridin-2-yl-amino] -propanoic acid Ethyl ester Methanesulfonate and | |
| ATE550329T1 (en) | HETEROBICYCLIC SULFONAMIDE DERIVATIVES FOR THE TREATMENT OF DIABETES | |
| NO20081482L (en) | Delta and epsilon crystal forms for imatinib mesylate | |
| DE602006010243D1 (en) | 4- (phenylamino) -6-oxo-1,6-dihydropyridazine-3-carboxamide derivatives as MEK inhibitors for the treatment of hyperproliferative disorders | |
| DK1725544T3 (en) | 3- [4-Heterocyclyl-1,2,3-triazol-1-yl] -N-aryl-benzamides as inhibitors of cytokine production for the treatment of chronic inflammatory diseases | |
| DK2051976T3 (en) | 4- [5-Methoxy-6- (2-methyl-6 [1,2,4) triazol-1-yl-pyridin-3-ylamino) -pyrimidin-4-yloxy] -piperidine-1-carboxylic acid isopropyl ester as modulator of metabolism and treatment of disorders related thereto | |
| IL192241A0 (en) | Improved process for the preparation of 4-(benzimidazolylmethylamino)-benzamides and the salts thereof | |
| DK1888033T3 (en) | Method and composition for the treatment of inflammatory diseases | |
| NO20054396D0 (en) | 3-methyl-2- (3- (2-phenyl-oxazol-4-ylmethoxy) -cyclohexanecarbonylamino) -morbic acid derivatives and similar compounds as PPAR modulators for the treatment of type 2 diabetes and atherosclerosis | |
| DK1817282T3 (en) | Suitable phenoxy derivatives for the treatment of respiratory diseases | |
| DE602007010303D1 (en) | USE OF 3- (4-AMINO-1-OXO-1,3-DIHYDRO-ISOINDOL-2-YL) -PIPERIDINE - 2,6-DION FOR THE TREATMENT OF COAT CLIMB | |
| DK1948176T3 (en) | Diarylurines for the treatment of pulmonary hypertension | |
| ATE538114T1 (en) | 4-(PYRIDINE-4-YL)-1H-Ä1,3,5UTRIAZINE-2-ONE DERIVATIVES AS GSK3 BETA INHIBITORS FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES | |
| DK1734959T3 (en) | Compounds for the treatment of schizophrenia and / or glucoregulatory abnormalities | |
| DE602006014300D1 (en) | METHOD AND SYSTEM FOR MEDIA-INDEPENDENT HANDOVER USING THE OAMP PROTOCOL | |
| UA100364C2 (en) | BIPHENYL-2-YLCARBAMIC ACID SUCCINATE 1- $ 2- (2-CHLORINE-4 - {$ (R) -2-HYDROXY-2- (8-HYDROXY-2-OXO-1,2-DYHYDROHYNOLYL) 5 ] METHYL]} - 5-METHOXYPHENYLCARBAMOYL) ETHYL] PIPERIDINE-4-IL-ESTER AND ITS USE FOR THE TREATMENT OF PULMONARY DISORDERS | |
| BRPI0810957A2 (en) | "medicated plaster comprising 5-methyl-1-phenyl-2- (1h) pyridone". | |
| DK1846354T3 (en) | Substituted cyclopentanes or cyclopentanones for the treatment of ocular hypertensive conditions | |
| WO2006102426A3 (en) | Methods for avoiding edema in the treatment of metabolic, inflammatory, and cardiovascular disorders | |
| DK2024354T3 (en) | 1 - [(4- [benzoyl (methyl) amino] -3- (phenyl) butyl] azetidine derivatives for the treatment of gastrointestinal disorders 1 |